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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499420Generated: November 3, 2026

Pyridine → HCID 86726672, compound

https://huagongshe.com/reaction/1499420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
Reactant2-(2,6-Difluorophenyl)-1,3-thiazole-4-carboxylic acidHCID 24278454—
ReactantHCID 86726669HCID 86726669—
SolventDichloromethaneHCID 6344—
ProductHCID 86726672HCID 8672667295.1%

Reaction Steps

A solution of 1-chloro-N,N,2-trimethylpropenylamine (114.1 mg, 0.8539 mmol) in DCM (1.0 mL) was added slowly to a suspension of 2-(2,6-difluorophenyl)-1,3-thiazole-4-carboxylic acid (Example 2, Step 2, 74.2 mg, 0.308 mmol) in DCM (1.0 mL). The mixture was stirred at room temperature for 2 h. A solution of tert-butyl {(3S)-1-[5-amino-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl]piperidin-3-yl}carbamate (125.1 mg, 0.2653 mmol) in DCM (2.0 mL) was added, followed by pyridine (217.3 mg, 2.747 mmol), and the mixture was then stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by chromatography on silica gel (0-100% EtOAc in hexanes) to give the sub-title compound as a dark oil (175.3 mg, 95%). LCMS calc. for C33H33F2N6O5S2 (M+H)+: m/z=695.2. found 695.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-fc094ecdc9ab4cf4ae5012c2af6c4247
Source noteuspto-grants-2015_12